Skip to content

Feasibility of predicting the timing of ventilator withdrawal using diaphragmatic ultrasound combined with peak expiratory flow rate

Feasibility of predicting the timing of ventilator withdrawal using diaphragmatic ultrasound combined with peak expiratory flow rate

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075138
Enrollment
Unknown
Registered
2023-08-25
Start date
2023-08-31
Completion date
Unknown
Last updated
2023-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

weaning

Interventions

ATRC group:SBT using ATRC mode
CPAP group:SBT using CPAP mode
PSV group:SBT using PSV mode

Sponsors

Central People's Hospital of Zhanjiang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1: Meet the conditions for conducting SBT: a. The primary disease is under control; b. Respiratory rate = 35 beats/min;c. Adequate oxygenation is defined as at least 90% (a small amount of inhaled oxygen [FIO2] = 40%, PEEP = 8cmH2O) or at least 150 PaO2/FIO2 (PEEP = 8cmH2O);d. Adequate coughing;e. Awakening state, defined as the Richmond Agitation and Sedation Scale (RASS) -2 to+1;f. Do not use continuous sedatives; g. Do not use vasopressors (or use the minimum dose) Can pass the 3-minute SBT screening test, which, like the SBT method, only conducts a 3-minute tolerance test. Patients with positive screening results will officially enter the trial stage;patients with negative screening results will be re screened 24 hours later to determine whether they have entered the trial phase. 2: The patient actively cooperates with all tests. 3: Informed consent from the patient's family.

Exclusion criteria

Exclusion criteria: 1: The condition is unstable and the SBT conditions have not been met yet 2: The patient is unwilling to cooperate with the examination 3: Patient and family members do not agree to the trial

Design outcomes

Primary

MeasureTime frame
Peak expiratory flow;Diaphragm excursion;Diaphragm excursion-time index;End inspiratory thickness of diaphragm;End expiratory thickness of diaphragm;Diaphragm thickening rate;

Countries

China

Contacts

Public ContactShiliang Ke

Central People's Hospital of Zhanjiang

haoyiksl@163.com+86 188 2610 8940

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026